Weight | 180.207 g/mol |
---|---|
Formula | C9H12N2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
Dulcin (150-69-6)
phenetolcarbamide · p-ethoxyphenylurea
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LabBot
- The genetics of tasting in mice. VI. Saccharin, acesulfame, dulcin and sucrose. (Genetics Research, 1989)
- Dulcin and Saccharin Taste in Squirrel Monkeys, Rats, and Men (Science, 1965)
- Studies on food additives. X. The metabolism of p-ethoxyphenylurea in the rabbit. (Chemical & Pharmaceutical Bulletin, 1966)
- Trennung, Nachweis und Bestimmung der knstlichen Sstoffe Cyclamat, Dulcin und Saccharin mittels Gas-Chromatographie (Fresenius Journal of Analytical Chemistry, 1971)
- Dnnschichtchromatographische Trennung und Identifizierung von Saccharin, Cyclamat und Dulcin (European Food Research and Technology, 1964)
- DERIVATIVES OF DULCIN (Journal of the American Chemical Society, 1931)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenetolcarbamide
- p-ethoxyphenylurea
-
SMILESCCOC1=CC=C(C=C1)NC(=O)N
-
InChIKeyGGLIEWRLXDLBBF-UHFFFAOYSA-N
- Pubchem - Dulcin
- Wikipedia - dulcin
Dulcin is an artificial sweetener about 250 times sweeter than sugar, discovered in 1883 by the Polish chemist Jzef (Joseph) Berlinerblau (27 August 1859 1935). It was first mass-produced about seven years later. Although it was discovered only five years after saccharin, it never enjoyed the latter compounds market success.
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Synthesis
Reactant
+
Ureidoradical
(Chan-Lam coupling reaction)
Reactant
+
ETHYL HYDROPEROXIDE
(Dakin oxidation)
Similar Compounds
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(6317-89-1)
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p-Nonyloxyaniline
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4-Octyloxyaniline
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p-Hexadecyloxyaniline
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p-Anisidine
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4-(2-(2-Methoxyethoxy)ethoxy)aniline
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m-Phenetidine
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N-(3,5-dimethoxyphenyl)acetamide
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